Middle to late Triassic mélange exhumation along a pre-Andean transpressional fault system: coastal Chile (26°–42° S)

Mélanges occur as discontinuous, mappable, units along an extensive N–S-trending, steeply dipping zone of distributed shear in metamorphic complexes along the coast of central Chile. Large mélange zones, from north to south, near Chañaral, Los Vilos, Pichilemu, and Chiloé Island, contain variations in lithologic and structural detail, but are consistent in exhibiting cross-cutting fabric features indicating a progressive transition from earlier ductile to more brittle deformation. In the Infiernillo mélange near Pichilemu, Permian to Early Triassic, sub-horizontal schistosity planes of the Western Series schist are disrupted, incorporated into, and uplifted along high-angle, N–S- to NNE–SSW-trending brittle–ductile shears. Mylonitic and cataclastic zones within the mélange matrix indicate active lateral shear during cumulative exhumation from depths exceeding 12 km in some areas. Exotic lithologies, such as Carboniferous mafic amphibolite and blueschist, formed during earlier Gondwanide subduction, match well with similar rocks in the Bahia Mansa to Los Pabilos region 750 km to the south, suggesting possible dextral offset. The development of the Middle to Late Triassic, N–S=trending, near-vertical shear zones formed weaknesses in the crust facilitating later fault localization, gravitational collapse, and subduction erosion along the continental margin. The length and linearity of this zone of lateral movement, coincident with a general hiatus of regional arc magmatism during the Middle to Late Triassic, is consistent with large-scale dextral transpression, or possible transform movement, during highly oblique NNE–SSW convergence along the pre-Andean (Gondwana) margin. The resultant margin parallel N–S-trending shear planes may be exploited by seismically active faults along the present coastal area of Chile. The palaeo-tectonic setting during the transitional period between earlier Gondwanide (Devonian to Permian) and later Andean (Late Jurassic to present) subduction may have had some similarity to the presently active San Andreas transform system of California.     

Biogeochemical evaluation of Nannorrhops ritchiana : A Mg-flora from Khuzdar, Balochistan, Pakistan

Nannorrhops ritchiana (Mazari Palm) is a distinctive flora growing in the Saharo-Sindian region. It is well distributed on the ultramafic soil, derived from the Bela Ophiolite in the Khuzdar District, Balochistan, Pakistan. Quantitative estimation of Ca, Mg, Fe and Ni in soil and plant ash has been carried out. The constituents of plant ash have been discussed in relation to soil chemistry, pH, climate, mobility, average abundance in plant ash and exclusion mechanism of the flora. Relationship among Ca, Mg, Fe and Ni has been established using scattergrams to evaluate the biogeochemistry of the plant. High contents of Mg and high coefficient of biological absorption allow it to be classed as Mg-flora. Both Ca and Fe appeared to be antagonistic to Mg. The metal assemblage ofN. ritchiana nicely reflected the nature of the bed rock as being serpentinized ultramafic, and its corresponding soils. Good exclusion mechanism ofN. ritchiana did not allow it to absorb high Ni from the soil. Relatively high concentrations of Ni inN. ritchiana from the Baran Lak area can be used to localize Ni-mineralization in the study area. Statistical analyses, such as minimum, maximum, mean, mode, median, standard deviations, and coefficient of correlation, were also made to improve raw geochemical data and interpretations.     

Geochemical Characterization of Bolivian Formative Earthen Architecture by Wavelength‐Dispersive X‐ray Fluorescence

In this study, we employ wavelength‐dispersive X‐ray fluorescence (WDXRF) to characterize construction materials from Formative civic architecture (1000 B.C.E.–C.E. 400), ethnographic mudbricks, and off‐site controls from the Taraco Peninsula, Bolivia. The preparation of earthen construction materials for civic buildings can shed light on aspects of community development such as labor organization, resource management, and architectural technologies. We apply geochemical results to reconstructing how public buildings were made as communities moved toward socio‐political complexity in this region. However, there are few geochemical studies in the Andes, and little prior scientific analysis of earthen architecture. We therefore tested the efficacy of WDXRF for this region, and developed control materials. Our archaeological samples were selected from two Formative villages, Chiripa and Kala Uyuni. In this study, we performed WDXRF analyses on 63 archaeological and control samples including archaeological floors, walling, plasters, and mortars, as well as contemporary ethnographic walling and topsoils. Elemental signatures for 28 elements clearly distinguished the archaeological flooring, walling, plaster, and mortars from ethnographic and off‐site controls. More subtle variations were detected that distinguish study sites and the different material types. Laboratory‐calibrated multi‐element XRF effectively supports efforts to reconstruct the pathways to social complexity in the Titicaca Basin.     

Fe- and Al-Rich metapelites of the Teiskaya Group, Yenisei Range: Geochemistry, protoliths, and the behavior of their material during metamorphism

The Fe- and Al-rich metapelite of the Teiskaya Group in the trans-Angara part of the Yenisei Range are characterized by variable P-T parameters of their metamorphism. Geochemical data on these rocks were used to reproduce the nature and composition of their protolith. The metapelites were determined to be redeposited and metamorphosed Precambrian weathering crusts of the kaolinite type, which were produced by the erosion of Archean rocks of predominantly acid (granitoid) composition in shallow-water continental-margin basins in a humid climate. These results are consistent with the results of the lithological-facies analysis and geodynamic reconstruction of the Precambrian geological evolution of complexes in the Yenisei range. Differences were revealed between the REE patterns in metapelites in various metamorphic zones caused by both the compositional heterogeneity of the protoliths and the prograde (in terms of pressure) mineral reactions of collision metamorphism with the predominant effects of various processes during different evolutionary stages.     

The effects of liquid immiscibility and thermal diffusion on oxygen isotopes in silicate liquids

Differences between the δ¹⁸O values of Si- and Fe-rich immiscible liquids in the system Fe₂SiO₄-KAlSi₂O₆-SiO₂ (Fa-Lc-Q) in isothermal experiments at 0.1 MPa have been determined experimentally to be 0.6 permil. The observed partition of ¹⁸O into the Si-rich liquid is consistent with previous experience with the preferential partition of ¹⁸O into Si-rich minerals in isothermal equilibrium with minerals of less polymerized structure. Crystallochemical principles affect the distribution of oxygen isotopes in coexisting isothermal liquids in the same way as they apply to isothermally coexisting crystals. The effects of Soret (thermal) diffusion on the distribution of oxygen isotopes in silicate liquids above the solvus in the system Fa-Lc-Q under conditions of an imposed temperature gradient of ca. 250 °C over 4 mm and at 2 GPa have also been investigated experimentally. Both the magnitude and the direction of separation of oxygen isotopes as a result of Soret diffusion are unexpected. For each of the silicate liquids, the cold end of the charge is enriched in ¹⁸O by up to 4.7 permil, and the highest δ¹⁸O values are associated with the most silica-poor compositions. The distribution of oxygen isotopes appears to be similar in each liquid, regardless of their chemical compositions, which is in contrast to the behaviour of cations whose distributions are compositionally dependent and characterized by strong crystallochemical effects wherein network-forming species such as Si and Al separate to the hot end and Mg, Fe and Ca are segregated preferentially to the cold end. Structural units in the melts are evidently less selective between oxygen isotopes than between cations, because oxygen redistribution over all possible sites in these units proceeds according to mass. Self-diffusion coefficients of oxygen in basaltic liquids estimated from the Soret experiments are in accord with those from other isotope tracer experiments, and comparable to those of Si. The possible effects of Soret diffusion on the oxygen isotopic composition of metasomatic veins in the mantle are examined in light of these data, and indicate that decay of the thermal gradients in the veins exceeds that of the diffusion of oxygen needed to produce variations in the δ¹⁸O values of mantle minerals. Variations in oxygen isotope ratios in most natural systems as a result of Soret effects are unlikely. Received: 6 January 1997 /  Accepted: 28 June 1998     

Mg-lattice associations in red coralline algae

Recent investigations have shown red coralline algae to record ambient temperature in their calcite skeletons. Temperature recorded by variation in Mg concentrations within algal growth bands has sub-annual resolution and high accuracy. The conversion of Mg concentration to temperature is based on the assumption of Ca replacement by Mg within the algal calcite skeleton at higher temperatures. While Mg-temperature relationships in coralline algae have been calibrated for some species, the location of Mg within the calcite lattice remains unknown. Critically, if Mg is not a lattice component but associated with organic components this could lead to erroneous temperature records. Before coralline algae are used in large scale climate reconstructions it is therefore important to determine the location of Mg. Synchrotron Mg-X-ray absorbance near edge structure (XANES) indicates that Mg is associated with the calcite lattice in Lithothamnion glaciale (contemporary free-living, contemporary encrusting and sub-fossil free-living) and Phymatolithon calcareum (contemporary free-living) coralline algae. Mg is deposited within the calcite lattice in all seasons (L. glaciale & P. calcareum) and thallus areas (P. calcareum). These results suggest L. glaciale and P. calcareum are robust Mg-palaeotemperature proxies. We suggest that similar confirmation be obtained for Mg associations in other species of red coralline algae aiding our understanding of their role in climate reconstruction at large spatial scales.     

Seasonal uranium distributions in the coastal waters off the Amazon and Mississippi Rivers

The chemical reactivity of uranium was investigated across estuarine gradients from two of the world’s largest river systems: the Amazon and Mississippi. Concentrations of dissolved (<0.45 μm) uranium (U) were measured in surface waters of the Amazon shelf during rising (March 1990), flood (June 1990) and low (November 1991) discharge regimes. The dissolved U content was also examined in surface waters collected across estuarine gradients of the Mississippi outflow region during April 1992, August 1993, and November (1993). All water samples were analyzed for U by isotope dilution inductively coupled plasma mass spectrometry (ICP-MS). In Amazon shelf surface waters uranium increased nonconservatively from about 0.01 μg I^?1 at the river’s mouth to over 3 μg I^?1 at the distal site, irrespective of river discharge stage. Observed large-scale U removal at salinities generally less than 15 implies a) that riverine dissolved U was extensively adsorbed by freshly-precipitated hydrous metal oxides (e.g., FeOOH, MnO₂) as a result of flocculation and aggregation, and b) that energetic resuspension and reworking of shelf sediments and fluid muds on the Amazon shelf released a chemically reactive particle/colloid to the water column which can further scavenge dissolved U across much of the estuarine gradient. In contrast, the estuarine chemistry of U is inconclusive within surface waters of the Mississippi shelf-break region. U behavior is most likely controlled less by traditional sorption and/or desorption reactions involving metal oxides or colloids than by the river’s variable discharge regime (e.g., water parcel residence time during estuarine mixing, nature of particulates, sediment storage and resuspension in, the confined lower river), and plume dispersal. Mixing of the thin freshwater lens into ambient seawater is largely defined by wind-driven rather than physical processes. As a consequence, in the Mississippi outflow region uranium predominantly displays conservative behavior; removal is evident only during anomalous river discharge regimes. ‘Products-approach’ mixing experiments conducted during the Flood of 1993 suggest the importance of small particles and/or colloids in defining a depleted U versus salinity distribution.